Stípek S, Mĕchurová A, Novák L, Trojan S
Faculty of Medicine, Charles University, Prague, Czechoslovakia.
Biomed Biochim Acta. 1989;48(2-3):S194-9.
Oxypurines (hypoxanthine + xanthine, HX) were measured polarographically in the mixed umbilical cord blood plasma, the maternal venous blood plasma and in the anterior amniotic fluid of 104 deliveries. The HX increase was found in groups with clinical signs of perinatal hypoxia. The HX concentration in the mixed umbilical plasma above 15 umol/l (i.e., means +/- 2 S.D.) should be considered as pathological. The following results of experiments on animals suggested a possible pathogenic significance of xanthine oxidase (XOD) reaction on hypoxic injury: The higher the plasma XOD activity of different species (guinea pig, hamster, rat, mouse) the shorter was the survival time of the species in the interrupted hypoxia. Administration of hypoxanthine decreased the survival time of rats in the interrupted hypoxia, while the administration of allopurinol increased it. Allopurinol suppressed the post-hypoxic autoimmune response of the rats to brain tissue.
在104例分娩的混合脐血血浆、母体静脉血血浆和羊膜前液中,采用极谱法测定了氧嘌呤(次黄嘌呤+黄嘌呤,HX)。在有围产期缺氧临床体征的组中发现HX升高。混合脐血浆中HX浓度高于15 μmol/l(即均值±2标准差)应被视为病理性的。以下动物实验结果提示黄嘌呤氧化酶(XOD)反应对缺氧损伤可能具有致病意义:不同物种(豚鼠、仓鼠、大鼠、小鼠)的血浆XOD活性越高,该物种在间歇性缺氧中的存活时间越短。给予次黄嘌呤会缩短大鼠在间歇性缺氧中的存活时间,而给予别嘌呤醇则会延长其存活时间。别嘌呤醇抑制了大鼠对脑组织的缺氧后自身免疫反应。